Class IITerminatedVoluntary: Firm initiated

Del Monte Fresh Produce N.A., Inc.: food recall F-0126-2025

Del Monte Fresh Produce N.A., Inc. of Jessup, MD recalled Del Monte Fresh Produce, Pineapple and Apple Salad 4/6.5oz plastic container, four containers per case. Refrigerated.… Reason: The product is being recalled due to an undeclared allergen - tree nuts (walnuts). The FDA listed it as Class II in its Enforcement Report dated Nov 20, 2024; distribution: Pennsylvania.

Record status as published: Terminated (terminated Nov 13, 2024). openFDA data last updated Oct 21, 2026.

Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.

Recall details

Product
Del Monte Fresh Produce, Pineapple and Apple Salad 4/6.5oz plastic container, four containers per case. Refrigerated. Lot Code 02277101, expiration date 10/10/2024 .
Product quantity
55 cases (220 Units).
Reason for recall
The product is being recalled due to an undeclared allergen - tree nuts (walnuts).
Codes, lots and dates on the package
Lot Code 02277101
Distribution pattern
All recalled products were distributed to one consignee in state. PA
Recalling firm
Del Monte Fresh Produce N.A., Inc., Jessup, MD
Classification
Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Voluntary or mandated
Voluntary: Firm initiated
How the firm first notified customers
E-Mail

Dates

EventDate
Recall initiated by the firmOct 8, 2024
Classified by the FDANov 8, 2024
Published in the Enforcement ReportNov 20, 2024
TerminatedNov 13, 2024

All food recall records

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Sources

  • U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0126-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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